Showing entry for Disorder of phenylalanine metabolism

General Disease Information
BXGD Id	BXGD005953
Disease Name	Disorder of phenylalanine metabolism
Disease CUI Id	C0268461
MeSH Codes	C16   C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations